4-(1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)morpholine
≥95%
- Product Code: 118477
CAS:
1206594-08-2
| Molecular Weight: | 329.24 g./mol | Molecular Formula: | C₁₉H₂₈BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22573395 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, its morpholine moiety can enhance solubility and bioavailability, making it valuable in designing drug candidates. The cyclopropyl group adds structural diversity, potentially contributing to the compound’s biological activity or stability in various applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,938.00 |
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| 0.250 | 10-20 days | ฿13,230.00 |
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| 1.000 | 10-20 days | ฿37,359.00 |
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4-(1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)morpholine
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, its morpholine moiety can enhance solubility and bioavailability, making it valuable in designing drug candidates. The cyclopropyl group adds structural diversity, potentially contributing to the compound’s biological activity or stability in various applications.
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